273
ABSTRACT
Exercise and apelin have been shown to increase cardiac function and elicit tolerance to ischemia/reper-fusion (IR) injuries. This study aimed at determining whether the combination of exercise training and apelin pretreatment could integrate the protective effects of each of them in the heart against IR injury. Male rats were divided into four experimental groups: 1: Rats with ischemia/reperfusion (IR), 2: subjected to exercise training for 8 weeks (EX+IR), 3: apelin-13 (10 nmol/kg/day) for 7 days (Apel+IR) in the last week of training, and 4: exercise training plus apelin-13 (EX+Apel+IR). Isolated hearts were perfused using the Langendorff method and subjected to 30 min of regional ischemia followed by 60 min of reperfusion. Treadmill exercise training was conducted for 8 weeks. Hemodynamic parameters were recorded throughout the experiment. Ischemia-induced arrhythmias, myocardial infarct size (IS), creatine kinase-MB (CK-MB) isoenzyme and plasma lactate dehydrogenase (LDH) activity was measured in all animals. Administration of apelin-13 plus exercise increased left ventricular developed pressure (LVDP) at the end of ischemia and reperfusion compared with other groups.
After 30 min of ischemia, dP/dtmax was higher in EX+Apel+IRthan in Apel+IR and EX+IR groups. During 30
min ischemia, exercise training, apelin-13 and combined treatment produced a significant reduction in the numbers of premature ventricular complexes. A combination of exercise and apelin-13 also reduced infarct size, CK-MB, LDH and severity of arrhythmia. These results suggest that combined therapies with apelin-13 and exercise training may integrate the beneficial effects of each of them alone on cardiac contractility, arrhythmia
and limiting of infarct size. Level of evidence I; Therapeutic Studies - Investigating the Results of Treatment.
Keywords: Exercise; Coronary reperfusion; Apelin- 13 peptide; Arrhythmias, Cardiac.
RESUMO
Foi demonstrado que o exercício e a apelina aumentam a função cardíaca e induzem a tolerância à lesões por isquemia/reperfusão (IR). O objetivo do presente estudo foi determinar se a combinação de treinamento físico e pré--tratamento com apelidos poderia integrar os efeitos protetores de cada um deles no coração contra a lesão por IR. Ratos machos foram divididos em quatro grupos experimentais: 1- Ratos com isquemia/ reperfusão (IR), 2- submeti-dos ao treinamento físico por 8 semanas (EX + IR), 3- apelino-13 (10 nmol / kg / dia) por 7 dias (Apel + IR) na última semana de treinamento, 4- treinamento físico mais apelina-13 (EX + Apel + IR). Corações isolados foram perfundidos pelo método de Langendorff e submetidos à 30 min de isquemia regional, seguida de 60 min de reperfusão. Treino em esteira foi conduzido por 8 semanas. Parâmetros hemodinâmicos foram registrados ao longo do experimento. Arritmias induzidas por isquemia, tamanho do infarto do miocárdio (IS), atividade da isoenzima Creatina Cinase-MB (CK-MB) e lactato desidrogenase plasmática (LDH) foram medidos em todos os animais. A administração de apelin-13 mais exercício aumentou a pressão desenvolvida pelo ventrículo esquerdo (LVDP) no final da isquemia e reperfusão em comparação com outros grupos. Após 30 min de isquemia, dp / dtmax foi maior em EX + Apel + IR do que nos grupos Apel + IR e EX + IR. Durante 30 min isquemia, treinamento físico, apelina-13 e tratamento combinado produ-ziram redução significativa no número de complexos ventriculares prematuros. Combinação de exercício e apelina-13 também reduziu o tamanho do infarto, CK-MB, LDH e gravidade da arritmia. Estes resultados sugerem que terapias combinadas com apelina-13 e treinamento físico podem integrar os efeitos benéficos de cada um deles sozinhos na contratilidade cardíaca, arritmia e limitação do tamanho do infarto. Nível de evidência I; Estudos terapêuticos - Investigação dos resultados do tratamento.
Descritores:Treino de exercícios; Reperfusão coronária; Apelina- 13 peptídeo; Arritmias Cardíacas.
RESUMEN
Se ha demostrado que el ejercicio y la apelina aumentan la función cardíaca y provocan tolerancia a las lesiones por isquemia/reperfusión (IR). Los objetivos del presente estudio fueron determinar si la combinación de entrenamiento con ejercicio y pre-tratamiento con apelina podrían integrar los efectos protectores de cada uno de ellos en el corazón frente a la lesión por IR. Los ratones machos se dividieron en cuatro grupos experimentales: 1: ratones con isquemia/ reperfusión (IR) 2: sometidos a entrenamiento durante 8 semanas (EX + IR), 3: apelina-13 (10 nmol / kg / día) durante
EFFECTS OF EXERCISE COMBINED WITH APELIN-13 ON
CARDIAC FUNCTION IN THE ISOLATED RAT HEART
EFEITOS DO EXERCÍCIO COMBINADO COM APELINA-13 NA FUNÇÃO CARDÍACA NO CORAÇÃO
ISOLADO DE RATOS
EFECTOS DEL EJERCICIO COMBINADO CON APELIN-13 EN LA FUNCIÓN CARDIACA DEL CORAZÓN
DE RATONES AISLADOS
Afshin Nazari1,2
(Physical Education Professional) Khadige Zahabi1
(Biologist) Yaser Azizi3
(Physical Education Professional) Maryam Moghimian4
(Physical Education Professional)
1. Lorestan University of Medical Sciences, Razi Herbal Medicines Research Center, Khorramabad, Iran. 2. Lorestan University of Medical, Department of Physiology, School of Medicine, Sciences, Khoramabad, Iran. 3. Iran University of Medical Sciences, Physiology Research Center, Department of Physiology, School of Medicine, Tehran, Iran. 4. Gonabad University of Medical Sciences, Department of Physiology, School of Medicine, Gonabad, Iran.
Correspondence:
Maryam Moghimian. Department of Physiology, School of Medicine, Gonabad University of Medical Sciences, Gonabad. Asian Road, Gonabad, Khorasan Razavi, I.R.IRAN. moghimian.m@gmu.ac.ir
ORIGINAL ARTICLE ARTIGO ORIGINAL
274
7 días (Apel + IR) en la última semana de entrenamiento 4: entrenamiento físico más apelina-13 (EX + Apel + IR). Los corazones aislados se perfundieron mediante el método de Langendorff y se sometieron a 30 minutos de isquemia regional, seguidos de 60 minutos de reperfusión. El entrenamiento de la cinta de correr se llevó a cabo durante 8 se-manas. Los parámetros hemodinámicos se registraron a lo largo del experimento. Se midieron las arritmias inducidas por isquemia, el tamaño del infarto de miocardio (IS), la isoenzima Creatina Kinase-MB (CK-MB) y las actividades de lactato deshidrogenasa plasmática (LDH) en todos los animales. La administración de ejercicios de apelina-13 plus aumenta la presión desarrollada del ventrículo izquierdo (PDVI) al final de la isquemia y la reperfusión en comparación con otros grupos. Después de 30 min de isquemia, la dp/dt max fue más alta en EX + Apel + IR que en los grupos Apel + IR y EX + IR. Durante la isquemia de 30 minutos, el entrenamiento físico, la apelina-13 y el tratamiento combinado, produjeron una reducción significativa en el número de complejos ventriculares prematuros. La combinación de ejercicio y apelina-13 también redujo el tamaño del infarto, CK-MB, LDH y la gravedad de la arritmia. Estos resultados sugieren que las terapias combinadas con apelina-13 y el entrenamiento físico pueden integrar los efectos beneficiosos de cada uno de ellos solo sobre la contractilidad cardíaca, la arritmia y la limitación del tamaño del infarto.Nivel de Evidencia I; Estudios terapéuticos - Investigación de los resultados del tratamiento.
Descriptores:Entrenamiento de ejercicio; Reperfusión coronaria; Apelina-13 péptido; Arritmias Cardiacas.
INTRODUCTION
The main pathological manifestation of coronary artery disease as a cause of death worldwide is myocardial damage due to ischemia/
reperfusion (IR) injury.1 In this regards many approaches to provide
cardioprotection against IR induced injury have been studied. Until now, regular exercise has been agreed to be a pragmatic and sustainable
countermeasure for cardioprotection.2 Exercise training is associated
with an increased myocardial perfusion capacity and with normal or
increased contractile function in the normal heart.3 It has been shown
that early aerobic exercise training reduced cardiac dysfunction after
myocardial infarction (MI) in trained rats4 and one of the most potent
stimuli for eliciting tolerance to IR injury is exercise.5 Additionally, animal studies have shown that aerobic exercise (both short-term and
long-term) confers cardioprotection against all levels of IR induced injuries.6
The beneficial effects of exercise on cardiac function can be attributed to an exercise-induced upregulation of endothelial nitric oxide (NO)
synthase (eNOS) expression and activity.7 Endogenous NO mediates the
cardioprotective effects of exercise in the setting of myocardial I/R injury.8
Apelin as an endogenous ligand of the human G-protein-coupled
receptor APJ5 plays an important regulatory role in cardiovascular
ho-meostasis.5,8 Apelin/APJ demonstrate significant hypotension and positive
inotropic action and are involved in signaling pathways implicated in
numerous cardiac and vascular functions.9 The Apelin-APJ system may
be involved in cardioprotection during acute myocardial ischemia.10 Its
cardioprotection against IR injury occurs through activation of PI3K/Akt/
eNOS and ERK signaling pathways.7
Involvement of apelin-13 in stabilizing cell membranes of the myo-cardium, reducing formation of reactive oxygen species (ROS), regulating expression of superoxide dismutase (SOD) and eNOS were demonstrated
in IR of rat heart in vivo.11 Phosphorylation and activation of eNOS are
also implicated in myocardial protection afforded by apelin.1,12
These findings suggest that the beneficial effects of exercise and apelin are only in part overlapping and thus partly complementary and although both apelin and aerobic exercise training have been highly recommended to the treatment of heart failure (HF), it is unknown whether the combination of aerobic exercise training and apelin has integrative effects on the treatment of myocardial IR injuries. To date, to the best of our knowledge there are no studies testing the combined effect of these two therapeutic strategies on cardiac function.
In view of the complementary mechanisms by which exercise and apelin appear to exert beneficial effects, we tested the hypothesis that
Article received on 01/28/2017 accepted on 12/08/2017 DOI: http://dx.doi.org/10.1590/1517-869220182404175002
combined treatment with exercise and apelin could exerts possible added benefit on IR injures in the isolated rat heart.
MATERIALS AND METHODS
28 male Wistar rats (200 –250 g) were obtained from Lorestan Uni-versity of Medical Sciences.
All experiments were conducted in accordance with the institutional guidelines of Lorestan University of Medical Sciences (Lorestan, Iran) and the National Institutes of Health guidelines for the care and use of labo-ratory animals (NIH Publication No. 85–23, revised 1996). All applicable institutional guidelines for the care and use of animals were followed (the protocol number of the Ethics committee: Lums.rec.1394.51).
Experimental groups
All of the hearts were subjected to 30 min ischemia and 60 min reperfusion.
Rats were randomly assigned to one of four experimental groups. IR: Ischemia/reperfusion; EX+IR: rats exposed to exercise training on the treadmill for 8 weeks; Apel+IR: apelin-13 was administered (10 nmol/kg/ day, ip) for 7 days once a day, and EX+Apel+IR: apelin-13 was administered (10 nmol/kg/d) for 7 days in the last week of training program (Diagram1) Diagram 1. Illustration of the experimental groups. Animals in con-trol group (IR) were subjected to 30 min ischemia followed by 60 min reperfusion by the Langendorff method and saline (NS) was administered intravenously before ischemia, (EX+IR group) rats exposed to exercise training on the treadmill for 8 weeks and saline was administered intra-venously before ischemia, (Apel+IR group) Apelin-13 was administered (10 nm/kg/day,ip) for 7 days prior to ischemia once a day,( EX+Apel+IR groups) rats exposed to exercise training on the treadmill for 8 weeks and Apelin-13 (10 nmol/kg/day,i.p.) for 7 days prior to ischemia once a day. NS, normal saline; TTC, triphenyltetrazolium chloride. (Figure 1)
Exercise training protocol
275
and exercise was stopped for 5 min. After this resting period, animals restarted to run till they reached an overall daily exercising time of 50 min. The exercise intensity was moderate and 55–60 % of maximal oxygen
consumption.13 The exercise training was performed 5 days per week
for 8 weeks. The determination of treadmill speed and exercise duration
was based on the previous studies.13
Langendorff model of myocardial I/R injury
Adult male rats were given 500 U of heparin by intraperitoneal. Anesthesia was achieved by administration of sodium thiopental (60 mg/kg, i.p.). Hearts were then excised and perfused retrogradely via the aorta at a constant pressure (80 mmHg) with oxygenated Krebs – Henseleit bicarbonate buffer, pH 7.4 at 37ºC. Heart function (ventricular balloon) was monitored throughout the experiments. For HR monitor-ing, electrocardiogram recording was made by fixation of thin stainless steel electrodes on the ventricular apex and right atrium. Isolated hearts underwent 20-min stabilization, then 30-min regional ischemia (induced by tightening the left anterior descending coronary artery) and 60-min reperfusion. Following the reperfusion period, the perfusion solution was collected for assessment of CK-MB and LDH release.
Infarct size measurement
After completion of the reperfusion period, the left coronary artery was reoccluded, and Evans blue dye was infused via the aorta to dif-ferentiate the ischemic zone (area at risk, AAR) from the non-ischemic zone. Hearts were frozen overnight at -20º C and then sliced, using a stainless steel rat heart slicer matrix with 2 mm coronal section slice intervals, into 2 mm transverse sections from apex to base. Slices were then incubated with 1% triphenyl tetrazolium chloride (TTC in 0.1 M phosphate buffer, pH= 7.4) for 20 min at 37 º C.TTC reacts with viable
tissue, producing a red formazan derivative, which is distinct from the white necrotic tissue once it is fixed in 10% formalin for 24 h. The areas of the left ventricle AAR and infracted tissue were measured by planim-etery from the scanned hearts by using the Photoshop program. AAR was expressed as a percentage of left ventricular size for each heart, and the infarct size (IS) was expressed as a percentage of AAR .
Biochemical analysis
The levels of CK-MB and LDH activity were assessed in coronary ef-fluent samples at 60 min of reperfusion with a specific CK-MB and LDH kit (Pars Azmoon, Tehran, Iran), using an auto analyzer (Roche Hitachi Modular DP Systems, Mannheim, Germany). The sensitivities of the as-says for CK-MB and LDH were 2-1000 IU/L and 0-1000 IU/L, respectively.
Evaluation of ischemic-induced arrhythmias
Ischemia-induced ventricular arrhythmias were determined in ac-cordance with the Lambeth conventions . In this regard, three forms of ventricular arrhythmias were analyzed as below: ventricular ectopic beat (VEB), was identified as premature QRS complex, ventricular tachycardia (VT) was defined as four or more seriate VEBs, ventricular fibrillation (VF), was characterized as undetectable QRS complex. Multipart forms of VEBs such as bigemi and salvos (couplet and triplet) were counted at separate episodes. The incidence, time of occurrence and duration of arrhythmias were used to identify arrhythmias severity according to the following scor-ing system ; 0: 0–49 VEBs, 1: 50–499 VEBs, 2: >499 VEBs and/or 1 episode of spontaneously reverting VT or VF, 3: >1 episode of VT or VF or both with a total duration <60 s, 4: VT or VF or both 60–120 s total duration, 5: VT or VF or both >120 s duration, 6: fatal VF starting at >15 min after occlusion, 7: fatal VF starting between 4 and 14 min 59 s, 8: fatal VF starting between 1 and 3min 59 s, 9: fatal VF starting <1 min after occlusion.
Figure 1. Illustration of the experimental groups. Animals in control group (IR) were subjected to 30 min ischemia followed by 60 min reperfusion by the Langendorff method and
saline (NS) was administered intravenously before ischemia, (EX+IR group) rats exposed to exercise training on the treadmill for 8 weeks and saline was administered intravenously before ischemia, (Apel+IR group) Apelin-13 was administered (10 nm/kg/day,ip) for 7 days prior to ischemia once a day,( EX+Apel+IR groups) rats exposed to exercise training on the treadmill for 8 weeks and Apelin-13 (10 nmol/kg/day,i.p.) for 7 days prior to ischemia once a day. NS, normal saline; TTC, triphenyltetrazolium chloride.
IR (Control group)
EX + IR
Apel + IR
EX + Apel + IR
-1 week 0 15 min 45 min 105 min
-1 week 0 15 min 45 min 105 min -8 week -1 week 0 15 min 45 min 105 min
-8 week -1 week 0 15 min 45 min 105 min Baseline
(15 min)
Baseline (15 min)
Baseline (15 min)
Baseline (15 min) Exercise training
(8 week)
Exercise training (8 week)
Ischemia (30 min)
Ischemia (30 min)
Ischemia (30 min)
Ischemia (30 min)
Reperfusion (60 min)
Reperfusion (60 min)
Reperfusion (60 min)
Reperfusion (60 min)
Infarct size analysis
Infarct size analysis
Infarct size analysis
Infarct size analysis
Intraventricular pressure recording
TTC
TTC
TTC
TTC NS
NS
Apelin
276
Statistical analysis
The hemodynamic parameters were analyzed using repeated mea-surement of analysis of variance (ANOVA) with treatment and exercise as grouping factors and time as a repeated factor followed by Tukey’s post hoc test. Differences in infarct size, CK-MB, and LDH were evaluated by one-way ANOVA (exercise and treatment as factors). When significant interaction was found, Tukey’s post hoc test was used for comparison between pair groups. Arrhythmia scores were analyzed with Kruskal–Wal-lis test followed by post hoc test Mann–Whitney, and the incidences of VT or VF was compared by Fisher exact test. All data were expressed as mean ± S.E.M. Statistical significance was defined as p < 0.05.
RESULTS
Cardiac function data observed at the baseline, end of ischemia and reperfusion in all groups are reported in Table 1.Since HR and LVDP may recover to different degrees, rate pressure product (RPP) was calculated by multiplying HR by LVDP and presented as a reliable left ventricular function parameter for the isolated heart. In baseline period, all hearts had a similar RPP, LVDP and coronary flow (CF). Apelin-13 induced a decrease of HR in baseline when compared with IR group (P<0.05). LVDP was decreased significantly at the end of ischemia and reperfusion in comparison with their baseline in all groups (all p<0.05). Moreover administration of apelin-13 plus exercise training was able to increase LVDP at the end of ischemia (both P<0.01) and reperfusion compared with EX+IR and Apel+IR (P<0.001 and P<0.05 respectively, Figure 2). dp/ dt max was decreased significantly at the end of ischemia and
reper-fusion in comparison with their baseline in IR,Apel+IRand EX+Apel+IR
groups (p<0.05). dp/dt max was lower at the end of reperfusion period
in comparison with their baseline in IR and Apel+IRgroup (both p<0.05).
There was significant increase of dp/dt max in EX+Apel+IR at the end of ischemia compared with other groups (all P<0.01). Administration of apelin-13 and exercise training alone had no significant effect (Figure 3). As shown in Table 1neither apelin-13 nor exercise training nor combined treatment elicited any effect whatsoever in RPP.
Area at Risk and Infarct Size
As shown in Figure 4, Area at Risk was similar between experimental groups. Statistical analysis showed that Exercise training followed by apelin-13 administration significantly decreased infarct size in EX+Apel+IR group compared to IR and EX+IR groups (both P<0.05).
BIOCHEMICAL ANALYSIS
CK-MB and LDH in coronary effluent
Exercise training followed by apelin-13 administration significantly decreased CK-MB and LDH levels in coronary effluent compared to control group (13.5±2.2 vs.30.6±8.8 and 10±2.5 vs. 41.2±14 respectively, both p<0.05). LDH levels also showed a significant decrease in EX+Apel+IR group compared with EX+IR and Apel+IR groups (10±2.5 vs. 60±9.8 and 36± 6 respectively, both p<0.05). EX+IR group promoted a higher increase in LDH than Apel+IR group (p<0.05, Figure 5A, 5B).
Ischemia-induced arrhythmias
Figure 6 shows electrocardiogram recording during baseline, coronary artery occlusion, ventricular ectopic beat (VEB), couplet, bigeminy; (F) ventriculartachycardia (VT) and ventricular fibrillation (VF).
Severity of arrhythmias
The results of exercise training, apelin-13 and combined treatment on ischemia-induced arrhythmias are shown in Figure 7.
Arrhythmia severity was significantly lower in hearts of AP+IR, EX+IR and EX+AP+IR During 30 min ischemia compare with IR group (all P<0.05).
Table 1. Hemodynamic parameters.
Group
Baseline End of ischemia30’ End of reperfusion60’
HR (bpm)
LVDP mmHg
RPP
bpm.mmHg CF (ml/min)
HR (bpm)
LVDP Basal value%
RPP Basal value%
CF (ml/min)
HR (bpm)
LVDP Basal value%
RPP Basal value%
CF (ml/min)
IR 326±16 82±5.1 26732±912.3 6±0.6 269±48 80±4&# 80±10 4±0.4 273±37 71±4&# 70±22 3±0.4&
EX+IR 326±15 81±4 26406±1095 6.3±0.6 343±12 72±3&# 90±15 2.8±0.6 330±164 70±3&# 80±11.6 2.8±0.4&
Apel+IR 209±29* 85±3.3 17765±514.5 7.4±1.1 205±31 72±3&# 80±13.5 4.2±0.6 265±359 72±3&# 64±9.5 3±0.8&
EX+Apel+IR 263±24 95±7 24985±1277 5.8±0.7 291±21 83±4& 91±16.4 3.2±0.3 291±35 80±5& 90±7.9 2.6±0.3&
Apel, apelin-13; bpm, beat per minute; CF, coronary flow; IR, ischemia reperfusion; HR, heart rate; LVDP, left ventricular developed pressure; EX, exercise; RPP, rate pressure product; Data are presented as mean±S.E.M. &P<0.05 vs.
baseline. *P<0.05 vs. IR group, #P<0.05 vs. EX+Apel+IR group.
Figure 2. LVDP, Left ventricular developed pressure at the end of reperfusion in different
groups (n = 8). EX, exercise; IR, ischemia–reperfusion; Apel, apelin. Data are presented as mean ± S.E.M. *P<0.05 compared to IR group, # P<0.01 compared to EX+IR group, & P<0.01 compared to Apel+IR group.
Figure 3. dp/dt in different groups (n = 8). EX, exercise; IR, ischemia–reperfusion; Apel,
apelin. Data are presented as mean ± S.E.M. & P<0.05 compared to baseline. # P<0.01 compared to EX+Apel+IR group.
IR EX + IR Apel + IR EX + Apel + IR
Baseline Isch Rep IR EX + IR Apel + IR EX + Apel + IR
LVDP%
277 Incidences of VT and VF.
No significant differences were observed in ventricular tachycardia (VT) and ventricular fibrillation (VF) incidences among groups (Figure 8).
The Numbers of (premature ventricular complex ) PVC
During 30 min ischemia, exercise training, apelin-13 and combined treatment produced a significant reduction in the numbers of PVC (all P<0.05, Figure 9).
DISCUSSION
Combined treatment was able to decrease infarct size and it also caused a significant decreased in arrhythmia and increase in LVDP of
EX+Apel+IRgroup compared with IR, EX+IRand Apel+IR groups at the
end of ischemia and reperfusion periods. Unexpectedly either treatment alone had no effect on cardiac function.
Previous studies have shown the beneficial effect of resistance
exercise on cardiac performance in heart failure patients.2
Moreover previous studies have demonstrated that exercise training
can protect against IR injury in clinical patients and rats.14
Soufi et al. showed that chronic resistance exercise also provides
cardioprotection against myocardial injuries.15 Contrary our findings
showed that exercise training alone unexpectedly had no effect on cardiac
function. These results are consistent with the findings of Barauna et al.16
Figure 4. The ratio of area at risk to total left ventricular areas (AAR/LV%) and ratio of
infarct size to area at risk (IS/AAR) in different groups (n = 8). AAR, area at risk; IS, infarct size; EX, exercise; IR, ischemia–reperfusion; Apel, apelin. Data are presented as mean ± S.E.M. * P < 0.05 compared to IR group, # P<0.05 compared to EX+IR group.
Figure 5. Levels of CK-MB (A) and LDH (B) in coronary effluent at the end of reperfusion
period in different groups (n = 8). EX, exercise; IR, ischemia–reperfusion; Apel, apelin. Data are presented as mean ± S.E.M. * P < 0.01 compared to IR group, # P<0.05 compared to EX+IR group, & P<0.05 compared to EX+Apel+IR group, $ P<0.05 compared to EX+IR group.
Figure 6. Shows electrocardiogram recording during baseline, coronary artery occlusion,
ventricular ectopic beat (VEB), couplet, bigeminy; (F) ventriculartachycardia (VT) and ventricular fibrillation (VF).
Figure 7. Distribution of the arrhythmia score during 30 min ischemia in different
groups (n = 8). EX, exercise; IR, ischemia–reperfusion; Apel, apelin. Data are presented as mean±S.E.M. *P < 0.05 compared to IR group.
Figure 8. Incidence of ventricular tachycardia (VT) and ventricular fibrillation (VF) during
30 min ischemia in different groups (n = 8). EX, exercise; IR, ischemia–reperfusion; Apel, apelin. Data are presented as mean±S.E.M.
IR EX + IR Apel + IR EX + Apel + IR
ST elevation
VT
VF
A B C
D E F
G
IR EX + IR Apel + IR EX + Apel + IR
IR EX + IR Apel + IR EX + Apel + IR
IR EX + IR Apel + IR EX + Apel + IR IR EX + IR Apel + IR EX + Apel + IR
R
atio (%)
AAR IS
CK
-MB (IU/L)
A
rr
h
ythmia sc
or
e
Incidenc
e (%)
A
B
LDH IU/L
278
who reported that 12 weeks of resistance training did not change cardiac function in the rats. Since it is reported that both duration and intensity of exercise may be significant factors in accomplishing exercise-induced
cardioprotection,17 they are likely to be more severe and therefore, need
more time for normalization to occur.
It has been previously shown that the apelin may also be a new and potentially important cardioprotective autacoid, which is up-regulated
rap-idly after myocardial ischemia.18,19 The endogenous apelin/APJ system is an
intrinsic protective pathway in IR injury.10 Apelin is involved in the regulation of vascular tone. Recent researches have shown that after administration of the apelin in rats decreases blood pressure and potentiates cardiac function.9 But hypotension is not the unique response to the administration of apelin in vivo. Kagiyama et al. has been reported that intravenous injections of 20 and 50 nmol of apelin-13 induce dose-dependent increases in arterial
pressure and heart rate in conscious rats.20 In our study apelin-13 injection
was followed by a decrease in heart rate at the baseline without changes in both LVDP and RPP in the isolated perfused rat heart preparation. Such decrease may attribute to reduced sympathetic discharge and an increase in the baroreceptor stimulation or both.
The mechanisms mediating the protective effects of apelin may be
through up-regulating eNOS.12 Furthermore Zeng et al. illustrated the
antiapoptotic effects of apelin/APJ in protecting against IR injury in the
heart.12 Recent studies have suggested that endogenous apelin/APJ
signaling participated in hypoxic retinal vascularization.21,22 Szokodi et al. showed that the inotropic response to apelin may involve activation of
phospholipase c (PLC), protein kinase c (PKC), and sarcolemmal Na+-H+
exchange (NHE) and Na+-Ca2+ exchange (NCX).9
In contrast to these findings the present study did not identify reduced infarct size induced by apelin-13. Earlier studies have reported infusion
of apelin induced a dose-dependent positive inotropic effect9 and in
the isolated rat heart, the size of a MI was significantly reduced.22 On the
contrary, it remained unchanged when apelin was given before ischemia by Rastaldo et al. suggesting that apelin mimics postconditioning (PostC)
rather than preconditioning (PreC).23 The reason for the lack of significant
effect of the apelin on infarct size is unclear, but we think It is likely that the ineffectiveness of apelin before ischemia is due to dose of apelin and its short half-life.24 Hence the different effect seems to depend on the different isoforms or dose of apelin. It is probably with a longer time of treatment and larger number rats these values could reach the statistical significance. The present study is the first to show in an experimental model, that unlike single treatments a dual treatment combining apelin-13 and exercise training attenuates heart function loss at the end of ischemia and reperfusion period and caused a significant increase in LVDP.
Although IR-induced myocardial injury occurs due to the complex interaction of numerous factors, increased production of ROS plays a major
role in IR-induced cardiac injury. Hence it is not surprising that
overexpres-sion of myocardial antioxidants minimizes IR- induced myocardial injury.25
In this context previous study revealed that apelin decreased ROS generation and MDA content and increased SOD activity and involved in the upregulation of lipid peroxidation in ex vivo and in vivo models of
myocardial IR injury26 suggesting that apelin/APJ may protect the heart
by reducing oxidative injury during IR. Also it was indicated that apelin could improve IR-induced cardiac dysfunction through increased NO formation and the action of apelin-12 in myocardial protection against
IR damage involved NO-dependent mechanisms.27 Nitric oxide (NO) is
known to be a potent vasodilator and antioxidant.
On the other hand physiological mechanisms for endurance training-induced cardioprotection against ischemia-reperfusion injuries have not been precisely understood, but it has been suggested that some mechanisms such as alterations in coronary circulation, expression of endoplasmic reticulum stress proteins, increased cyclooxygenase-2 activity, induction of myocardial heat shock proteins, improved cardiac antioxidant capacity and elevation of ATP-sensitive potassium channels may be involved in this cardioprotection.18,28 In this regard, Chicco et al.8 have reported that 6 week resistance exercise protected against alcohol-induced myocardial stress by enhancing antioxidant defense. Develop-ment of collateral coronary blood vessels could also play a significant role in providing cardioprotection against IR-induced myocardial injury
and chronic exercise can promote angiogenesis in some animal model.22
Therefore the positive functional effect of combined treatment with apelin-13 and exercise training in this study stems in part from specific regulation of the signaling pathway involving NO dependent mecha-nisms protecting cardiac myocytes against IR-induced oxidative stress. In our study, combined treatment with apelin-13 and exercise training was able to further decreases infarct size compared to apelin-13 treat-ment or exercise training applied solely that is in agreetreat-ment with earlier study showing that high intensity interval training for 30 min per day can protect the heart against IR injury and decreases infarct size nearly
by 50 % compared to sedentary group.29
Despite of effects of apelin-13 and exercise alone on cardiac func-tion, infarct size and biochemical parameters, our results showed that both single treatments and exercise training plus apelin-13 prevent IR-induced arrhythmias which is in agreement to findings of Powers
et al.18 and Hamilton et al.30 That observed antiarrhythmic protection in
exercised hearts during 20 min ischemic insult. It should be noted that the major effects of cardioprotection are reduction of infarct size (anti necrotic effect), reduction of number and severity of cardiac arrhythmias (anti arrhythmic effect) and improvement of contractile performance (protection against contractile dysfunction). Apelin-13 plus exercise training improved contractile function, reduced IR induced arrhythmias and releasing of CK-MB and LDH which was in the same direction with the infarct size in our experiment. Elevated level of CK-MB has been regarded as a specific biochemical marker of myocyte necrosis and LDH level, plays an important role in systemic tissue damage.
Taken together, we provided evidence that combined therapies with apelin-13 and exercise training may integrate the beneficial effects of isolated ones on heart rate, PVC, cardiac contractility and limiting of infarct size. The molecular mechanisms underlying the beneficial effects of combined therapies may relate to reduced myocardial oxidative stress.
ACKNOWLEDGEMENTS
This study was supported by the grant of Tehran University of Me-dical Science.
All authors declare no potential conflict of interest related to this article
Figure 9. The numbers of premature ventricular complex (PVC) during 30 min ischemia
in different groups (n = 8). EX, exercise; IR, ischemia–reperfusion; Apel, apelin. Data are presented as mean±S.E.M. *P < 0.05 compared to IR group.
IR EX + IR Apel + IR EX + Apel + IR
279
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AUTHORS’ CONTRIBUTIONS: Each author made significant individual contributions to this manuscript. AN (0000-0002-1863-1092)*, KZ (0000-0001-7878-1124)*, YA
